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Furthermore, when a side chain and/or a peptide amino terminal and/or a peptide carboxy terminal of each amino acid residue constituting the glutathione derivative of the present invention or a salt thereof has been chemically modified or protected, peptide synthesis is followed by chemical modification, or peptide synthesis is performed using a chemically modified amino acid, or an appropriate reaction condition is selected for the final deprotection of peptide synthesis, as described in a method conventionally known in the art of peptide synthetic chemistry ("Peputidogosei no Kiso to Jikken (Basic and Experimental Peptide Synthesis)" (Nobuo Izumiya, Tetsuo Kato, Haruhiko Aoyagi, Michinori Waki: Maruzen), "Zoku Iyakuhinno Kaihatsu - Dai 14 Kan - Peputido gosei (Development of Pharmaceuticals, Second series, Vol
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Weight:0.1mg
Curr Pharm Des 16: 1224–34
